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Specificity of Anti-Citrullinated Protein Antibodies in Rheumatoid Arthritis

Rheumatoid arthritis (RA) is an autoimmune disease of unknown etiology. The majority of individuals with RA are positive for the disease-specific anti-citrullinated protein antibodies (ACPAs). These antibodies are primarily of cross-reactive nature, hence, the true autoantigen to ACPA remains uniden...

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Autores principales: Trier, Nicole H., Holm, Bettina E., Hansen, Paul R., Slot, Ole, Locht, Henning, Houen, Gunnar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6640722/
https://www.ncbi.nlm.nih.gov/pubmed/31544843
http://dx.doi.org/10.3390/antib8020037
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author Trier, Nicole H.
Holm, Bettina E.
Hansen, Paul R.
Slot, Ole
Locht, Henning
Houen, Gunnar
author_facet Trier, Nicole H.
Holm, Bettina E.
Hansen, Paul R.
Slot, Ole
Locht, Henning
Houen, Gunnar
author_sort Trier, Nicole H.
collection PubMed
description Rheumatoid arthritis (RA) is an autoimmune disease of unknown etiology. The majority of individuals with RA are positive for the disease-specific anti-citrullinated protein antibodies (ACPAs). These antibodies are primarily of cross-reactive nature, hence, the true autoantigen to ACPA remains unidentified. In this study, we analyzed the reactivity of RA sera to several post-translationally modified epitopes, in order to further characterize the specific nature of ACPAs by immunoassays. Substituting citrulline with other amino acids, e.g., D-citrulline, homo-citrulline and methyl-arginine illustrated that ACPAs are utmost specific for citrullinated targets. Collectively, these findings support that ACPAs and citrullinated targets are specific for RA, making citrulline-containing peptide targets the most effective assays for detection of ACPAs.
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spelling pubmed-66407222019-09-05 Specificity of Anti-Citrullinated Protein Antibodies in Rheumatoid Arthritis Trier, Nicole H. Holm, Bettina E. Hansen, Paul R. Slot, Ole Locht, Henning Houen, Gunnar Antibodies (Basel) Article Rheumatoid arthritis (RA) is an autoimmune disease of unknown etiology. The majority of individuals with RA are positive for the disease-specific anti-citrullinated protein antibodies (ACPAs). These antibodies are primarily of cross-reactive nature, hence, the true autoantigen to ACPA remains unidentified. In this study, we analyzed the reactivity of RA sera to several post-translationally modified epitopes, in order to further characterize the specific nature of ACPAs by immunoassays. Substituting citrulline with other amino acids, e.g., D-citrulline, homo-citrulline and methyl-arginine illustrated that ACPAs are utmost specific for citrullinated targets. Collectively, these findings support that ACPAs and citrullinated targets are specific for RA, making citrulline-containing peptide targets the most effective assays for detection of ACPAs. MDPI 2019-06-07 /pmc/articles/PMC6640722/ /pubmed/31544843 http://dx.doi.org/10.3390/antib8020037 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Trier, Nicole H.
Holm, Bettina E.
Hansen, Paul R.
Slot, Ole
Locht, Henning
Houen, Gunnar
Specificity of Anti-Citrullinated Protein Antibodies in Rheumatoid Arthritis
title Specificity of Anti-Citrullinated Protein Antibodies in Rheumatoid Arthritis
title_full Specificity of Anti-Citrullinated Protein Antibodies in Rheumatoid Arthritis
title_fullStr Specificity of Anti-Citrullinated Protein Antibodies in Rheumatoid Arthritis
title_full_unstemmed Specificity of Anti-Citrullinated Protein Antibodies in Rheumatoid Arthritis
title_short Specificity of Anti-Citrullinated Protein Antibodies in Rheumatoid Arthritis
title_sort specificity of anti-citrullinated protein antibodies in rheumatoid arthritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6640722/
https://www.ncbi.nlm.nih.gov/pubmed/31544843
http://dx.doi.org/10.3390/antib8020037
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